Benzo(a)quinolizidine derivatives

ABSTRACT

An antiphlogistic compound of the formula (I) ##STR1## or a pharmaceutically effective salt thereof wherein R 1  and R 2  are hydrogen or C 1-4  alkoxy or together form a methylenedioxy group; 
     R 3 , R 4 , R 5 , and R 6  are hydrogen or a group of the formula --CH 2  --(CH 2 ) n  -R 7  with the proviso that at least one of R 3 , R 4 , R 5  and R 6  is other than hydrogen; 
     R 7  is a carboxylic group or a carboxylic acid derivative group; n=0, 1 or 2, provided that if R 3 , R 4  and R 5  are hydrogen and R 7  in the group R 6  is cyano or alkoxycarbonyl, and n=1, then R 1  and R 2  are hydrogen, C 2-4  alkoxy, or together form a methylenedioxy group.

This application is a continuation-in-part of copending Ser. No. 624,470 filed Oct. 21, 1975 now U.S. Pat. No. 4,102,886.

This invention related to benzo(a)quinolizidine derivatives, pharmaceutical compositions comprising the same, and a method of treatment using compounds of the invention.

According to the present invention there are provided benzo(a)quinolizidine derivatives of the formula (I) ##STR2## and salts thereof having an antiinflammatory therapeutic effect, wherein R¹ and R² each are hydrogen or a C₁₋₄ alkoxy group, or together form a methylenedioxy group;

R³, R⁴, R⁵ and R⁶ may be the same or different and are hydrogen or a group of the formula --CH₂ --(CH₂)_(n) -R⁷ provided that at least one of the symbols R³, R⁴, R⁵ and R⁶ is other than hydrogen;

R⁷ stands for a carboxyl group or a carboxylic acid derivative group; and

n=0.1 or 2.

In Hungarian Pat. Nos. 153,695 and 155,959 compounds of the formula (I) are disclosed, wherein R¹ and R² are hydrogen or alkoxy, R³, R⁴ and R⁵ are hydrogen, R⁶ is a group of the formula --CH₂ --(CH₂)_(n) -R⁷ is cyano- or alkoxycarbonyl and n=1. According to these patents such compounds are prepared by reacting 3,4-dihydroisoquinoline with quaternary salts or unsaturated ketones. Thus compounds of the above type are described in which R¹ and R² are methoxy.

According to the process of the present invention the compounds of the formula (I) ##STR3## having the formula (II) ##STR4## (wherein R and n=0 or 1) by reacting a compound of the formula (III) ##STR5## with a compound of the formula (IV) ##STR6## (wherein R¹⁰ is a cyano- or alkoxycarbonyl with C, to C₇ alkoxy). In the compound thus obtained the R¹⁰ group can be converted into an R⁷ group by hydrolysis, ammonolysis, halogenating and/or esterification. The compound of the formula (I) or (II) can be converted into a pharmaceutically effective salt thereof.

The term "carboxylic acid derivative group" as used herein encompasses all usual carboxylic acid derivative groups, e.g. alkoxycarbonyl (e.g. methoxycarbonyl, etc.), phenoxycarbonyl, phenylalkoxycarbonyl, carbonyl halide (e.g. carbonylchloride), carbamoyl or substituted carbamoyl groups. The carbamoyl group may be substituted by alkyl (e.g. methyl, ethyl, etc.) aryl (e.g. phenyl) groups. The carboxylic acid derivative group may be a N-heterocyclic carbonyl group (e.g. morpholinocarbonyl group) or an aralkylcarbamoyl group (e.g. benzylaminocarbonyl group).

The terms "alkyl group" and "alkoxy group" used throughout the specification relate to straight or branched chained group having 1-7, preferably 1-4 carbon atoms (e.g. methyl, methoxy, ethyl, ethoxy, n-propyl, isopropoxy, etc.).

In accordance with the invention an alkoxycarbonyl or a nitrile group may be converted into other groups, i.e. a group R¹⁰ may be converted into a group R⁷. Thus an alkoxycarbonyl or nitrile group may be converted into a carboxyl, halogenocarbonyl, or optionally substituted carbamoyl (alkyl-, aryl or aralkylsubstituted carbamoyl) or N-heterocyclic carbonyl (e.g. morpholinocarbonyl) group.

The said subsequent reactions may be carried out by methods known per se. Thus an alkoxycarbonyl group may be converted into a carboxyl group by hydrolysis or reacted with the corresponding amines. The acid amides may also be prepared by reacting a free carboxylic acid with a halogenating agent (e.g. thionylchloride) and reacting the acid halide thus obtained with the corresponding amine.

The compounds of the formula (I) may be transformed into salts of an inorganic acid (e.g. hydrochloric acid, hydrobromic acid, etc.) or organic acids (e.g. acetic acid, citric acid, etc.). Salt formation may also be carried out by methods known per se. One may proceed preferably by reacting a compound of the formula (I) with the solution of the corresponding acid formed with alcohol.

According to a further aspect of the present invention, there are provided a method of treatment and pharmaceutical compositions having antiinflammatory effect comprising as active ingredient a compound of the formula (I) or a salt thereof. ##STR7## wherein R⁷ is a carboxylic group of a carboxylic acid derivative group;

with the further proviso that if R³, R⁴ and R⁵ are hydrogen and R⁷ in the R⁶ is cyano or alkoxycarbonyl and n=1, then R¹ and R² are hydrogen, C₂₋₄ alkoxy, or together form a methylenedioxy group in admixture with suitable inert solid or liquid carriers.

The pharmaceutical compositions of the present invention may be prepared by methods of pharmaceutical industry known per se. The compositions may be put up in solid (e.g. tablets, pills, coated pills, etc.) and liquid (e.g. solution, emulsion and suspension) form. The composition may be suitable for oral, parenteral and rectal administration. The inert diluents may be starch, calcium carbonate, magnesium stearate, magnesium carbonate, water, polyalkyleneglycol, etc.

The dosage of the active ingredient may vary within a wide range and depends on the requirements of the given case. Generally it may be stated that the daily dosage of the active ingredient of the formula (I) may be from about 300 mg to about 500 mg. It is preferred to use the compositions in a dosage unit formed by tablets or capsules comprising from about 50 mg to about 150 mg of a compound of the formula (I).

The benzo(a)quinolizidine derivatives of the formula (I) possess valuable pharmacological effects, and can be used primarily as potent antiphlogistic agents for animal subjects. In the following there are summarized the pharmacological tests performed with the compounds of the formula (I), and the results of these tests. The compounds examined in the pharmacological tests were represented by the following symbols: [see formula (II)]

    ______________________________________                                         Symbol    R.sup.1   R.sup.2   R.sup.7  n                                       ______________________________________                                         SC 118    --O--CH.sub.2 --O--                                                                            CN         1                                         SCT-1     --OCH.sub.3                                                                              --OCH.sub.3                                                                              CN       1                                       SCT-2     --OCH.sub.3                                                                              --OCH.sub.3                                                                              CH.sub.3 COO--                                                                          1                                       SCT-3     --OC.sub.2 H.sub.5                                                                       --OC.sub.2 H.sub.5                                                                       CN       1                                       ______________________________________                                    

As evidenced by the results of the different tests, the benzo(a)quinolizidine derivatives of the formula (I) possess the same or even more potent antiphlogistic effect than phenylbutazone.

Inhibition of kaolin- and carrageenin-induced oedema

The tests are carried out on groups each consisting of at least 10 animals. The percentage inhibition of oedema, in relation to the untreated controls, was determined for each of the animals, and the average values were calculated. These average values are listed in Table 1 below.

                  TABLE 1                                                          ______________________________________                                                                        INHIBITION OF                                                     INHIBITION   CARRA-                                                            OF KAOLIN-   GEENIN-                                                           INDUCED      INDUCED                                                           OEDEMA 2     OEDEMA 1.5                                              DOSAGE    HOURS AFTER  HOURS AFTER                                     COM-    MG/KG     ADMINIS-     ADMINIS-                                        POUND   P.O.      TRATION, %   TRATION, %                                      ______________________________________                                         SC 118  25        18.1.sup.+   22.0.sup.+                                              50        27.5.sup.+   30.6.sup.++                                             75        43.7.sup.++  47.7.sup.++                                             100       53.4.sup.++  52.7.sup.++                                     SCT-1   25        20.5.sup.+   --                                                      50        21.4.sup.+   24.2.sup.+                                              75        24.8.sup.+   25.7.sup.+                                              100       47.8.sup.++  37.7.sup.++                                     SCT-2   25        5.8          --                                                      50        21.4.sup.+   14.3                                                    75        24.7.sup.+   2.8                                                     100       --           17.0                                            SCT-3   25        17.3.sup.+   25.1.sup.+                                              50        19.4.sup.+   41.5.sup.++                                             75        48.9.sup.++  --                                                      100       45.9.sup.++  53.7.sup.++                                     Phenyl-                                                                        butazone                                                                               50        27.5.sup.++  24.3.sup.+                                      Indo-                                                                          methacine                                                                              10        27.2.sup. ++ 26.7.sup.+                                      Na-                                                                            salicylate                                                                             100       10.5         16.2                                            ______________________________________                                          .sup.+ P = 0.01                                                                .sup.++ P = 0.05 (significance levels according to Student's "t" test)   

                  TABLE 2                                                          ______________________________________                                         Cotton granuloma test                                                                      Dosage                                                             Compound    (mg/kg)      Effect, %                                                                               p                                            ______________________________________                                         SC 118      50           26.4     0.01                                         Phenylbutazone                                                                             50           19.6     0.05                                         Na-salicylate                                                                              100          25.5     0.05                                         ______________________________________                                    

The benzo(a)quinolizidine derivatives according to the invention exert outstandingly high activities in the inhibition of serotonine-induced oedema, superseding many times the activities of phenylbutazone and indomethacine.

Tests performed on serotonine-induced oedema

The tests were carried out on groups each consisting of 10 animals. The percentage inhibition of oedema, in relation to the untreated controls, was determined for each of the animals. The data listed in Table 3 are the averages of the inhibition values.

                  TABLE 3                                                          ______________________________________                                                      Dosage     Percentage inhibition                                  Compound     (mg/kg) p.o.                                                                              1 hour after admin.                                    ______________________________________                                         SC 118       25         28.5.sup.+                                                          50         42.1.sup.+                                                          75         48.7.sup.+                                             SCT-1        50         22.4.sup.+                                                          100        57.8.sup.+                                             SCT-2        100        16.0                                                   SCT-3        50         36.2.sup.+                                                          100        47.0.sup.+                                             Phenylbutazone                                                                              100        10.2                                                   Indomethacine                                                                               25         1.4                                                    ______________________________________                                          .sup.+ P = 0.001 (Student's "t" test)                                    

Besides their antiphlogistic activities, some of the benzo(a)quinolizidine derivatives have antipyretic effects as well.

On the basis of the tests performed on experimentally provoked fever, the antipyretic activities of the compounds according to the invention surpass the effect of amidazophenum.

Antipyretic activity

                  TABLE 4                                                          ______________________________________                                                 Dosage Variation of body temperature                                           mg./kg.                                                                               1         2         3                                           Compound  p.o.     hours after administration                                  ______________________________________                                         SC-118    50       -2.75.sup.+++                                                                            -3.34.sup.+++                                                                          -4.03.sup.+++                                       25       -1.67.sup.+++                                                                            -1.81.sup.+++                                                                          -1.60.sup.++                              Phenylbutazone                                                                           50       -1.05.sup.++                                                                             -1.07.sup.++                                                                           -0.76.sup.30                                        25       -0.82.sup.++                                                                             -0.84.sup.++                                                                           -0.73.sup.+                               Amidazo-  25       -1.17.sup.+++                                                                            -0.94.sup.++                                                                           -0.95.sup.++                              phenum                                                                         ______________________________________                                          .sup.+ p = 0.05                                                                .sup.++ p = 0.01                                                               .sup.+++p = 0.001                                                        

Furthermore, as evidenced by the results of the hotplate and writhing tests, the compounds according to the invention possess analgesic effects as well. In this respect the compounds according to the invention are superior to phenylbutazone.

Examination of the analgesic effect by the hot-plate test

                  TABLE 5                                                          ______________________________________                                                   Dosage                                                                         mg./kg.   Prolongation of the reaction time,                         Compound  p.o.      % (2 hours after administration)                           ______________________________________                                         SC-118    50        61.2                                                       SCT-2     50        26.4                                                       SCT-3     50        33.9                                                       Indomethacine                                                                            50        no evaluable effect can be                                 Phenylbutazone                                                                           50        observed                                                   ______________________________________                                    

Examination of the analgesic effect by the writhing test

                  TABLE 6                                                          ______________________________________                                                 Dosage                                                                         mg./kg.  Activity, % (reduction of the number                          Compound                                                                               p.o.     of writhings in relation to the controls)                     ______________________________________                                         SC-118  50       41.8                                                          Phenyl- 100      17.6                                                          butazone                                                                       ______________________________________                                    

Besides the antiphloggistic and antipyretic effects, the new benzo(a)quinolizidine derivatives also have a sedative effect on the central nervous system.

Narcosis Potentiating effect

                  TABLE 7                                                          ______________________________________                                                   Dosage    Prolongation of the sleep period                                     mg./kg.   in relation to the untreated                               Compound  p.o.      controls, %                                                ______________________________________                                         SC-118    50        253.0                                                                25        96.4                                                       SCT-1     50        207.6                                                                25        132.8                                                      SCT-2     50        28.3                                                       SCT-3     50        240.2                                                                25        131.7                                                      Meprobamate                                                                              20        110.2                                                      ______________________________________                                    

The results of the toxicity examinations indicate that most of the benzo(a)quinolizidine compounds according to the invention have about the same degree of toxicity as phenylbutazone.

Acute toxicity tests

The acute toxicity values of the compounds were determined on rats, after oral administration. The LD₅₀ values were calculated according to the Litchfield-Wilcoxon method. The results are summarized in Table 8.

                  TABLE 8                                                          ______________________________________                                         Compound       LD.sub.50 mg./kg. p.o.                                          ______________________________________                                         SC-118         1407.63                                                         SCT-1          620                                                             SCT-3          780                                                             Aspirin        1700                                                            Phenylbutazone 1181.45                                                         Indomethacine  12                                                              ______________________________________                                    

In order to give a more detailed information, in the following there are given the results of the toxicity tests performed with compound SC-118. The tests were carried out on CFY rats, each weighing 150 to 200 g.

                  TABLE 9                                                          ______________________________________                                                Dead animals/treated animals                                                   48 hours                                                                Dosage after administration                                                    mg./kg.                                                                               m        f        m     f     m     f                                   ______________________________________                                          750   0/10     0/10     0/10  0/10  0/10  0/10                                1000   1/10     2/10     2/10  2/10  2/10  2/10                                1250   2/10     3/10     3/10  3/10  3/10  3/10                                1500   5/10     6/10     5/10  6/10  5/10  6/10                                1750   6/10     6/10     8/10  8/10  8/10  8/10                                2000   10/10    10/10    10/10 10/10 10/10 10/10                               ______________________________________                                          LD.sub.50 m = 1425 mg./kg.                                                     LD.sub.50, f = 1400 mg./kg.                                                    m = male                                                                       f = female                                                               

When examining the subtoxic effects it appeared that none of the compounds according to the invention exert ulcerogeneous effects or harmful influence on the haematopoietic system, either. As a comparison it should be noted e.g. indomethacine has a marked ulcerogeneous effect.

Determination of ulcer index

                  TABLE 10                                                         ______________________________________                                                     Ulcer      Erosion                                                 Compound      male   female    male female                                     ______________________________________                                         SC-118        0/10   0/10      0/10 0/10                                       SCT-1         1/10   2/10      3/10 4/10                                       SCT-3         1/10   0/10      6/10 4/10                                       Control       0/10   0/10      0/10 0/10                                       Indomethacine 3/10   3/10      1/10 1/10                                       Phenylbutazone                                                                               3/10   1/10      0/10 0/10                                       Na-salicylate 4/10   2/10      1/10 3/10                                       ______________________________________                                    

Thus the benzo(a)quinolizidine derivatives of the formula (I) are substances with significant antiphlogistic effects, possessing valuable antipyretic and analgesic activities as well. The sedative effects of these compounds are also not negligible. Moreover, these compounds are completely devoid of the undesired side-effects (e.g. ulcerogeneous effect) charcteristic of the nonsteroidal antiphlogistic agents, and their therapeutical indices are far more favorable than that of indomethacine.

Therapeutical indices

                  TABLE 11                                                         ______________________________________                                                    Therapeutical index LD.sub.50 /ED.sub.50                            Compound     kaolin-oedema                                                                              carrageenin-oedema                                    ______________________________________                                         SC-118       29.2        22.6                                                  SCT-1        12.4        6.7                                                   SCT-3        15.0        19.8                                                  Indomethacine                                                                               2.3         1.3                                                   ______________________________________                                    

Based on the above, the compound according to the invention can be used as antiphlogistic and analgesic agents primarily in the treatment of disorders evoked by the inflammation of joints and skeletal musculature.

Because of their non-ulcerogeneous character and of the lack of harmful side-effects on the haematopietic system, these compounds can also be administered for a prolonged period, which is very desirable in the treatment of the abovementioned disorders.

EXAMPLE 1 2-Oxo-3-(β-methylcarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

1.0 g. (4.98 mmoles) of 4-dimethylaminomethyl-5-oxo-capric acid methyl ester are added to a solution of 1.0 g. (4.95 mmoles) of 9,10-methylenedioxy-isoquinoline hydrochloride in 3 ml. of distilled water, and the reaction mixture is allowed to stand for one day. The separated substance is filtered off, and washed successively with water and methanol. 1.5 g. (92%) of 2-oxo-3-(β-methoxycarbonylethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine are obtained; m.p.: 123°-124° C. (after recrystallization from methanol).

Characteristic IR-bands (in KRr): 2750, 2800 cm⁻¹ (Bohlmann-bands), 1750 cm⁻¹ (CH₃ COO--) and 1740 cm⁻¹ (C═O).

NMR-spectrum (in deuterochloroform): τ=3.38 (C₁₁ --H), 3.42 (C₈ -H), 4.10 (--O--CH₂ --O--) and 6.30 (CH₃ COO--).

EXAMPLE 2 2-Oxo-3-(β-cyano-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

1.0 g. (5.92 mmoles) of 4-dimethylaminomethyl-5-oxo-capronitrile are added to a solution of 1.0 g. (4.95 mmoles) of 9,10-methylenedioxy-isoquinoline hydrochloride in 3 ml. of distilled water, and the mixture is allowed to stand for one day. The separated crystalline substance is filtered off, and washed successively with water and methanol. 0.9 g. (64%) of 2-oxo-3-(β-cyano-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)qunolizidine are obtained; m.p.: 154°-155° C. (after recrystallization from methanol).

Characteristic IR-bands (in KBr): 2380 cm⁻¹ (CN), 1715 cm⁻¹ (C═O), 2750, 2800 cm⁻¹ (Bohlmann-bands).

NMR-spectrum (in deuterochloroform): τ=3.48 (C₁₁ --H), 3.53 (C₈ --H) and 4.18 (--O--CH₂ --O--).

EXAMPLE 3 2-Oxo-3-(β-methoxycarbonyl-ethyl)-9,10-dimethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

1.0 g. of 4-dimethylaminomethyl-5-oxo-capric acid methyl ester is added to a solution of 1.0 g. (4.4 mmoles) of 9,10-dimethoxyisoquinoline hydrochloride in 3 ml. of distilled water, and the reaction mixture is allowed to stand for one day. The separated crystalline substance is filtered off, and washed successively with water and methanol. 1.45 g. (95%) of 2-oxo-3-(β-methoxycarbonyl-ethyl)-9,10-dimethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine are obtained; m.p.: 131° C. (see also Tetrahedron Letters 26, 2975 (1966).

EXAMPLE 4 2-Oxo-3-β-cyano-ethyl)9,10-dimethyoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

1.0 g. (5.92 mmoles) of 4-dimethylaminomethyl-5-oxo-capronitrile is added to a solution of 1.0 g. (4.4 mmoles) of 9,10-dimethoxyisoquinoline hydrochloride in 3 ml. of distilled water, and the reaction mixture is allowed to stand for one day. The separated substance is filtered off, and washed first with water and then with a small amount of methanol. 0.85 g. (62%) of 2-oxo-3-(β-cyano-ethyl)-9,10-dimethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine are obtained; m.p.: 130°-131° C. (see also Tetrahedron Letters 26, 2975 (1966).

EXAMPLE 5 2-Oxo-3-(β-carboxy-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

A mixture of 5.0 g. (15.1 mmoles) of 2-oxo-2-(β-methoxycarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine, 60 ml. of 10% hydrochloric acid and 40 ml. of methanol is heated on a steam bath for 3 hours. Thereafter the mixture is evaporated in vacuo to dryness, and the residue is recrystallized from a mixture of methanol and ether. 5.2 g. (98%) of 2-oxo-3-(β-carboxy-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine are obtained; m.p.: 196°-197° C.

Characteristic IR-bands (in KBr): 1715 cm⁻¹ (C═O), (COOH).

EXAMPLE 6 2-Oxo-3-(β-aminocarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

A mixture of 3.0 g. (9.0 mmoles) of 2-oxo-3-(β-methoxy-carbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine and and 50 ml. of a 10% methanolic ammonia solution is heated in a sealed tube at 100° C. for one day. Thereafter the mixture is evaporated t dryness, and the residue is recrystallized from methanol. 2.8 g. (98%) of 2-oxo-3-(β-aminocarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine are obtained; m.p.: 196°-197° C.

Characteristic IR-bands (in KBr): 3060, 3180 cm⁻¹ (NH), 2750-2800 cm⁻¹ (Bohlmann-bands), 1660-1690 cm⁻¹ (C═O, CONH₂).

EXAMPLE 7 2-Oxo-3-(β-chlorocarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

5.0 g. (42 mmoles) of thionyl chloride are reflux condensed, to 5.0 g. (14.2 mmoles) of 2-oxo-3-(β-carboxy-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine. During the addition the mixture is stirred vigorously. A strong gas evolution sets in. The mixture is heated on a steam bath for one hour, thereafter it is diluted with 20 ml. of dry benzene, and the obtained mixture is evaporated to dryness in vacuo. The residue is triturated with petroleum ether, and the solids are filtered off. 5.3 g. (100%) of 2-oxo-3-(β-chlorocarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine are obtained; m.p.: 110° C.

Characteristic IR-bands (in KBr): 1735, 1770 cm⁻¹ (C═O), (COCl).

EXAMPLE 8 2-Oxo-3-(β-benzoylaminocarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

0.5 g. (1.34 mmoles) of the acid chloride prepared as described in Example 7 are suspended in 15 ml. of dioxane, and 0.23 g. (2.68 mmoles) of triethylamine are added to the suspension. The reaction mixture is heated to 50° C. under stirring, and thereafter 0.143 g. (1.34 mmoles) of benzylamine are added. The reaction mixture is stirred at 50° C. for one hours, thereafter it is cooled to room temperature, filtered, and the filtrate is evaporated to dryness in vacuo. The residue is triturated with 10 ml. of water, the liquid is decanted, and 10 ml. of dry benzene are added to the solid. The benzene is evaporated in order to remove the last traces of water, and the residue is recrystallized from methanol, 0.45 g. (86%) of 2-oxo-3-(β-benzoylaminocarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine are obtained; m.p.: 188°-189° C.

Characteristic IR-bands (in KBr): 3230 cm⁻¹ (NH), 1695 cm⁻¹ (C═O), 1635 cm⁻¹ (CONH--).

NMR-spectrum (in deuterochloroform): τ=3.50, 3,56 (aromatic protons), 4.20 (--O--CH₂ --O--), 5.63, 5.73 (CH₂).

EXAMPLE 9 2-Oxo-3-(β-morpholinocarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

0.5 g. (1.34 mmoles) of the acid chloride prepared as described in Example 7 are suspended in a mixture of 3 ml. of absolute chloroform and 10 ml. of dioxane, and 0.35 g. (4.02 mmoles) of morpholine are added to the suspension. The reaction mixture is allowed to stand for one day and then the solution is extracted with 30 ml. of dichloromethane. The extract is dried, and evaporated to dryness. The residue is recrystallized from methanol. 0.35 g. (67.5%) of 2-oxo-3-(β-morpholinocarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine are obtained; m.p.: 168.5° C.

Characteristic IR-bands (in KBr): 2750, 2800 cm⁻¹ (Bohlmann-bands), 1700 cm⁻¹ (C═0), 1640 cm⁻¹ (CONH).

NMR-spectrum (in deuterochloroform): τ=3.50, 3.56 (aromatic protons), 4.20 (--O--CH₂ --O--), 6.49 (morpholine-protons).

EXAMPLE 10 2-Oxo-3-(β-diethylaminocarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

0.5 g. (1.34 mmoles) of the acid chloride prepared as described in Example 7 are suspended in a mixture of 3 ml. of chloroform and 10 ml. of dioxane, and 0.29 g. (4.08 mmoles) of diethylamine are added to the suspension. The reaction mixture is stirred at room temperature for one day. Thereafter the mixture is diluted with 30 ml. of water, and extracted with 30 ml. of chloroform. The chloroform phase is dried and evaporated to dryness. The residue is purified by preparative layer chromatography, converted into its hydrochloride, and the hydrochloride is crystallized from a mixture of methanol and ether. 0.25 g. (46.5%) of 2-oxo-3-(β-diethylaminocarbonyl-ethyl)-9,10-methylenedioxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine hydrochloride are obtained; m.p.: 175°-176° C.

Characteristic IR-bands (in KBr): 1730 cm⁻¹ (C═O), 1630 cm⁻¹ (CON).

EXAMPLE 11 2-Oxo-3-(β-methoxycarbonyl-ethyl)-9,10-diethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

1.0 g. (3.95 mmoles) of 9,10-diethoxyquinoline hydrochloride is dissolved in 3 ml. of distilled water, and 0.8 g. (3.98 mmoles) of 4-dimethylaminomethyl-5-oxo-capric acid methyl ester are added to the solution. The mixture is allowed to stand for one day. The separated crystals are filtered off, and washed successively with water and methanol. 1.4 g. (94.5%) of 2-oxo-3-(β-methoxycarbonyl-ethyl)-9,10-diethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)-quinolizidine are obtained; m.p.: 130°-132° C. (after recrystallization from methanol).

Characteristic IR-bands (in KBr): 2750, 2800 cm⁻¹ (Bohlmann-bands), 1730 cm⁻¹ (CH₃ COO-), 1715 cm⁻¹ (C═O).

EXAMPLE 12 2-Oxo-3-(β-cyano-ethyl)-9,10-diethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

1.0 g. (3.95 mmoles) of 9,10-diethoxyquinoline hydrochloride is dissolved in 3 ml. of distilled water, and 0.8 g. (4.75 mmoles) of 4-dimethylaminomethyl-5-oxo-capronitrile are added to the solution. The reaction mixture is allowed to stand for one day, thereafter the separated crystals are filtered off, and washed successively with water and methanol. 1.2 g. (89%) of 2-oxo-3-(β-cyanoethyl)-9,10-diethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine are obtained; m.p.: 135°-136° C. (after recrystallization from methanol).

Characteristic IR-bands (in KBr): 2750, 2800 cm⁻¹ (Bohlmann-bands), 2300 cm⁻¹ (CN), 1710 cm⁻¹ (CO).

EXAMPLE 13 2-Oxo-3-(β-cyano-ethyl)-9,10-dimethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

A mixture of 1.3 g. (3.82 mmoles) of 1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2,3-dehydro-2-pyrrolidino-11bH-benzo(a)quinolizidine, 10 ml. of anhydrous ethanol and 0.346 g. (1.7-fold amount) of acrylnitrile is heated to boiling for 8 hours, whereupon the reaction mixture is cooled and evaporated. The residue is shaken with a 2.5% sodium hydrogen carbonate solution and extracted five times with 10 ml. of ether each. The ether extract is dried, evaporated to dryness and the residue is crystallized from methanol. Thus 2-oxo-3-(β-cyano-ethyl)-1,2,3,4,6,7-hexahydro-9,10-dimethoxy-11bH-benzo(a)quinolizidine is obtained; m.p.: 131° C.

Characteristic IR bands (in KBr) 2750-2800 (Bohlmann-bands), 2270 (C.tbd.N), 1710 (C═0), 1605 cm⁻¹ (aromatic).

EXAMPLE 14 2-Oxo-1-(β-cyano-ethyl)-9,10-dimethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

A mixture of 0.535 g. (1.7 mmoles) of 1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2,3-dehydro-2-pyrrolidino-11bH-benzo(a)quinolizidine, 7 ml. of anhydrous benzene and 90 mg. (1.7 mmoles) of acryl nitrile is allowed to stand for 4 days, whereupon the reaction mixture is poured into water, separated, the benzene layer is dried and evaporated to dryness. The residue is separated on a KG-PF₂₅₄₋₃₆₆ plate by using a benzene-methanol (14-2) mixture. Elution is carried out with acetone. The product is obtained from the upper layer. The melting point of the 2-oxo-1-(β-cyano-ethyl)-9,10-dimethoxy-1,2,3,4,6,7-hexahydro-9,10-dimethoxy-11bH-benzo(a)quinolizidine amounts to 181°-182° C.

Analysis: for the formula C₁₈ H₂₂ N₂ O₃ (314,38): calculated: C, 68.76; H, 7.05; N, 8.91%; found: C, 68.14; H, 7.16; N, 9.22%.

Characteristic IR bands (in KBr) 2750-2800 (Bohlmann-bands) 2280 (CN), 1715 (C═O), 1620 cm⁻¹ (aromatic).

EXAMPLE 15 2-Oxo-bis(β-cyano-ethyl)-9,10-dimethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

A mixture of 0.9 g. (2.86 mmoles) of 1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2,3-dehydro-2-pyrrolidino-11bH-benzo(a)quinolizidine, 8 ml. of anhydrous ethanol and 0.58 ml. of acryl nitrile (3-fold amount) is heated to boiling for 4 hours. The reaction mixture is poured into 25 ml. of water, the precipitated crystals are filtered and heated to boiling with methanol. The melting point of the 2-oxo-bis (β-cyano-ethyl)-9,10-dimethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine amounts to 183°-184° C.

Analysis: for the formula C₂₁ H₂₅ N₃ O₃ (367.44): calculated: C, 48.64; H, 6.86; N, 11.43%; found: C, 68.00; H, 6.82; N, 11.60%.

Characteristic IR bands (in KBr) 2750-2800 (Bohlmann-bands), 2300 (C.tbd.N), 1715 (C═O), 1610 cm⁻¹ (aromatic).

EXAMPLE 16 2-Oxo-3-(β-methoxycarbonyl-ethyl)-9,10-dimethoxy-1,2,3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine

0.56 g. (1.78 mmoles) of 1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2,3-dehydro-2-pyrrolidino-11bH-benzo(a)quinolizidine are dissolved in 7 ml. of anhydrous benzene, whereupon 1.53 g. (1.78 mmoles) of methylacrylate are added and the reaction mixture is allowed to stand at room temperature for 4 days, whereupon it is poured into 50 ml. of water, the organic phase is dried, and evaporated to dryness. The residue is purified on a KG-PF₂₅₄₋₃₆₆ plate, as developing solvent a 14:2 mixture of benzene and methanol is used. The melting point of the 2-oxo-3-(β-methoxycarbonyl-ethyl)-1,2,3,4,6,7-hexahydro-9,10-dimethoxy-11bH-benzo(a)quinolizidine amounts to 131° C.

Characteristic IR bands (in KBr) 2750-2800 (Bohlmann-bands), 1737, 1700 (COOCH₃, CO), 1605 cm⁻¹ (aromatic).

EXAMPLE 17

The enamines are prepared as follows:

Into a flask equipped with a magnetic stirrer, 1.4 g. (5.35 mmoles) of 2-oxo-1,2,3,4,6,7-hexahydro-9,10-dimethoxy-11bH-benzo(a)quinolizidine, 10.5 ml. of pyrrolidine and 22 ml. of anhydrous benzene are added. The reaction mixxture is distilled off under nitrogen while stirring and anhydrous benzene containing 10% of pyrrolidine are added dropwise at a rate, which corresponds to the speed of distillation. After 5 hours the solution is evaporated to dryness. Thus amorphous 1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2,3-dehydro-2-pyrrolidino-11bH-benzo(a)quinolizidine is obtained. Characteristic IR bands (in KBr) 2750-2800 (Bohlmann-bands), 1650 (C═C, enol), 1605 cm⁻¹ (aromatic). The morpholino-derivative is obtained in an analogous manner. 

We claim:
 1. 2-oxo-3-(beta-cyano-ethyl)-9,10-methylenedioxy-1,2, 3,4,6,7-hexahydro-11bH-benzo(a)quinolizidine. 